Canonical Allele Identifier: CA2362531930
Gene: SRC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.37393674A= , CM000682.2:g.37393674A= GRCh38
NC_000020.10:g.36022077A= , CM000682.1:g.36022077A= GRCh37
NC_000020.9:g.35455491A= NCBI36
NG_023033.1:g.53990A= , LRG_1018:g.53990A=

Transcript Alleles

HGVS Amino-acid change
ENST00000358208.9:c.402-221A= ENSP00000350941.5:n.402-221A=
ENST00000692112.1:c.351-221A= ENSP00000508666.1:n.351-221A=
ENST00000692423.1:c.351-221A= ENSP00000509325.1:n.351-221A=
ENST00000373578.7:c.351-221A= MANE Select ENSP00000362680.2:n.351-221A=
ENST00000358208.8:c.351-221A= ENSP00000350941.4:n.351-221A=
ENST00000373558.2:c.369-221A= ENSP00000362659.2:n.369-221A=
ENST00000373567.6:c.351-221A= ENSP00000362668.2:n.351-221A=
ENST00000373578.6:c.351-221A= ENSP00000362680.2:n.351-221A=
ENST00000472968.1:n.182-221A=
NM_005417.4:c.351-221A= NP_005408.1:n.351-221A=
NM_198291.2:c.351-221A= , LRG_1018t1:c.351-221A= NP_938033.1:n.351-221A=
XM_011529013.1:c.351-221A= XP_011527315.1:n.351-221A=
XM_011529014.1:c.351-221A= XP_011527316.1:n.351-221A=
XM_011529013.2:c.351-221A= XP_011527315.1:n.351-221A=
XM_017028024.1:c.369-221A= XP_016883513.1:n.369-221A=
XM_017028025.1:c.369-221A= XP_016883514.1:n.369-221A=
XM_017028026.1:c.369-221A= XP_016883515.1:n.369-221A=
XM_017028027.2:c.369-221A= XP_016883516.1:n.369-221A=
NM_005417.5:c.351-221A= NP_005408.1:n.351-221A=
NM_198291.3:c.351-221A= MANE Select NP_938033.1:n.351-221A=